A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520453



Internal ID15447746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17603731..17634601hg38UCSC Ensembl
Innerchr11:17625278..17656148hg19UCSC Ensembl
Innerchr11:17581854..17612724hg18UCSC Ensembl
Innerchr11:17581854..17612724hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3830871
hg1930871
hg1830871
hg1730871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671583, nssv687020, nssv702588
Samples
Known GenesOTOG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520453
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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